19 results
·
20ms
·
Sources: EU EUDAMED, US FDA
SAS SHIGELLA SONNEI FORM I ANTISERUM (3/100/1000ML)
FDA 510(k)
FDA Class 2
·Microbiology
P.F.C. SIGMA
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295239451·P.F.C. SIGMA TC3 TIBIAL INSERT TRIAL SZ 3 20mm ...
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471149830·K-WIRE - DOUBLE TROCAR FULLY THREADED 1.5mm DIA...
Golden Isles Pedicle Screw System
FDA UDI
Intelivation, LLC·G079C1029615340·Cross Connector
PREFERENCE
FDA UDI
CTL Medical Corporation·00841732151130·Cross-connector 34mm Fixed
Preference 2
FDA UDI
SINTX Technologies, Inc.·M555102961534·34mm Fixed Cross Connector Assembly
EasyOne Pro Respiratory Analysis System
FDA 510(k)
FDA Class 2
·Anesthesiology
ZIEHM VISION FD DIGITAL MOBILE IMAGING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·February 28, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·October 26, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·August 22, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·November 28, 2023
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·April 18, 2023
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·September 25, 2024
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·October 15, 2025
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code GCL·October 1, 2024
CORAIL2 NON COL HO SIZE 11
FDA Adverse Event
Injury
·DEPUY FRANCE SAS - 3003895575·Product code KWA·February 14, 2013
TENDRIL STS
FDA Adverse Event
Death
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 28, 2014
COULTER® HMX HEMATOLOGY ANALYZER WITH AUTOLOADER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·January 14, 2011